QA Specialist

Medicareplus International Ltd; London; On-site; GBP 100,000 - 125,000; Full time

Job summary

A leading medical devices company in Wembley, London, seeks a Quality Assurance Specialist to enhance healthcare compliance and quality. The ideal candidate has proven experience in the Medical Devices industry and strong knowledge of ISO13485 regulations. Responsibilities include managing quality processes, ensuring compliance, and supporting audits. Join a dynamic team dedicated to improving patient outcomes and continuous professional development.

Benefits

Competitive salary

Collaborative work environment

Professional development opportunities

Contribution to patient outcomes

Qualifications

• Proven experience in a quality role within the Medical Devices industry.
• Up-to-date knowledge of ISO13485 regulations and other relevant regulatory frameworks.
• Exceptional attention to detail and capability to manage diverse data sources.

Responsibilities

• Maintaining and improving the ISO13485-compliant Quality Management System.
• Managing essential quality processes such as Document Control, Internal Audits, and CAPA.
• Analysing quality data, reviewing batch records, and managing customer complaints.

Skills

Attention to detail

Problem-solving

Analytical skills

Communication skills

Job description

Overview

Are you ready to make a difference in healthcare? Do you have an eye for detail and a passion for quality? Want to join a dynamic team dedicated to excellence and compliance?

We are currently looking for a Quality Assurance (QA) Specialist with proven experience in the Medical Devices industry and strong knowledge of ISO13485 regulations to join our busy team based in Wembley, London! This is an exhilarating opportunity to shape the future of healthcare compliance and quality assurance with a dedicated and innovative organisation.

Hours of Work: Full-time & On-site

Responsibilities

• Maintaining and improving the ISO13485-compliant Quality Management System
• Managing essential quality processes such as Document Control, Internal Audits, and CAPA
• Analysing quality data, reviewing batch records, and managing customer complaints
• Ensuring compliance with Medical Device Directives, Regulations, and International Standards
• Actively supporting internal and external audits to maintain regulatory excellence

Qualifications

• Proven experience in a quality role within the Medical Devices industry
• Up-to-date knowledge of ISO13485 regulations and other relevant regulatory frameworks
• Exceptional attention to detail and capability to manage diverse data sources
• Excellent organisational, problem-solving, and analytical skills
• Strong communication skills, both internally and with external partners

Benefits

• Competitive salary
• Opportunity to work in a collaborative and supportive environment
• Actively contribute to improving patient outcomes
• Professional development and continuous learning opportunities
• Become part of a dynamic healthcare organisation with a clear mission and values

Meet the Organisation: Who We Are and What We Do

At Medicareplus International, we are dedicated to delivering high-quality products that improve patient outcomes across the globe. Our commitment to quality and compliance is unwavering, and we take pride in fostering an environment where our team can thrive and innovate.

If you think you are suitable for this QA Specialist role, apply now and be part of a team making a meaningful impact in healthcare!